chrstartstopreference nucvariant nucdepthgenic statuszygosityvariant ID
104302336543023366G-3GENIChomozygous51434398
104302399643023997TC12GENIChomozygous51434399
104302492243024923CT17GENIChomozygous52190528
104302497543024979TTTT----7GENICpossibly homozygous52495682
104302499443024995GGT5GENIChomozygous52495684
104302513643025148AATGAATGAATG------------13GENIChomozygous51434404
104302542943025441CTCTCTCTCTCT------------7GENIChomozygous52495686
104302547343025482CCTCCTCCT---------3GENIChomozygous51434405
104302574343025744GGA5GENICheterozygous51434409
104302592543025926TC18GENIChomozygous51434410
104302593143025932TC17GENIChomozygous51434411
104302623343026234GA13GENIChomozygous51434412
104302692843026929AG16GENIChomozygous51434414
104302707043027071TC16GENIChomozygous51434415
104302963243029633TTC11GENIChomozygous51434416
104303012843030129AC13GENIChomozygous51434417
104303033743030338CCGT9GENICpossibly homozygous51434419
104303031343030315TG--10GENIChomozygous52317019